AR056196A1 - Arilamidas substituidas por dioxazina y por oxidiazina - Google Patents
Arilamidas substituidas por dioxazina y por oxidiazinaInfo
- Publication number
- AR056196A1 AR056196A1 ARP060103992A ARP060103992A AR056196A1 AR 056196 A1 AR056196 A1 AR 056196A1 AR P060103992 A ARP060103992 A AR P060103992A AR P060103992 A ARP060103992 A AR P060103992A AR 056196 A1 AR056196 A1 AR 056196A1
- Authority
- AR
- Argentina
- Prior art keywords
- carbon atoms
- alkyl
- alkoxy
- atoms
- carbon
- Prior art date
Links
- PPSZHCXTGRHULJ-UHFFFAOYSA-N dioxazine Chemical group O1ON=CC=C1 PPSZHCXTGRHULJ-UHFFFAOYSA-N 0.000 title 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 115
- 125000000217 alkyl group Chemical group 0.000 abstract 22
- 125000003545 alkoxy group Chemical group 0.000 abstract 17
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 abstract 7
- 125000001841 imino group Chemical group [H]N=* 0.000 abstract 7
- 125000003342 alkenyl group Chemical group 0.000 abstract 6
- 125000004644 alkyl sulfinyl group Chemical group 0.000 abstract 6
- 125000004390 alkyl sulfonyl group Chemical group 0.000 abstract 6
- 125000004414 alkyl thio group Chemical group 0.000 abstract 6
- 125000000304 alkynyl group Chemical group 0.000 abstract 6
- 125000001188 haloalkyl group Chemical group 0.000 abstract 6
- 229910052736 halogen Inorganic materials 0.000 abstract 6
- 150000002367 halogens Chemical class 0.000 abstract 6
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 5
- 125000004429 atom Chemical group 0.000 abstract 5
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 5
- 229910052799 carbon Inorganic materials 0.000 abstract 5
- 125000006310 cycloalkyl amino group Chemical group 0.000 abstract 5
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 5
- 125000004438 haloalkoxy group Chemical group 0.000 abstract 5
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 5
- 125000004665 trialkylsilyl group Chemical group 0.000 abstract 5
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 4
- 125000000262 haloalkenyl group Chemical group 0.000 abstract 4
- 125000004440 haloalkylsulfinyl group Chemical group 0.000 abstract 4
- 125000004441 haloalkylsulfonyl group Chemical group 0.000 abstract 4
- 125000004995 haloalkylthio group Chemical group 0.000 abstract 4
- 125000001424 substituent group Chemical group 0.000 abstract 4
- 125000003282 alkyl amino group Chemical group 0.000 abstract 3
- -1 amino, aminoformyl Chemical group 0.000 abstract 3
- 125000000232 haloalkynyl group Chemical group 0.000 abstract 3
- 125000005347 halocycloalkyl group Chemical group 0.000 abstract 3
- 229910052739 hydrogen Inorganic materials 0.000 abstract 3
- 239000001257 hydrogen Substances 0.000 abstract 3
- 125000004435 hydrogen atom Chemical class [H]* 0.000 abstract 3
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 3
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 2
- 125000001072 heteroaryl group Chemical group 0.000 abstract 2
- 238000000034 method Methods 0.000 abstract 2
- HCMJWOGOISXSDL-UHFFFAOYSA-N (2-isothiocyanato-1-phenylethyl)benzene Chemical compound C=1C=CC=CC=1C(CN=C=S)C1=CC=CC=C1 HCMJWOGOISXSDL-UHFFFAOYSA-N 0.000 abstract 1
- DXGMMGATZRQTEO-UHFFFAOYSA-N 2-amino-1-$l^{1}-oxidanylethanone Chemical compound NCC([O])=O DXGMMGATZRQTEO-UHFFFAOYSA-N 0.000 abstract 1
- 150000001204 N-oxides Chemical class 0.000 abstract 1
- JCXJVPUVTGWSNB-UHFFFAOYSA-N Nitrogen dioxide Chemical compound O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 abstract 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 1
- 241000607479 Yersinia pestis Species 0.000 abstract 1
- 235000019568 aromas Nutrition 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 1
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 abstract 1
- 125000002618 bicyclic heterocycle group Chemical group 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 239000013067 intermediate product Substances 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 239000001301 oxygen Substances 0.000 abstract 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- 239000000047 product Substances 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 229910052717 sulfur Inorganic materials 0.000 abstract 1
- 239000011593 sulfur Substances 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/88—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms six-membered rings with three ring hetero atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C259/00—Compounds containing carboxyl groups, an oxygen atom of a carboxyl group being replaced by a nitrogen atom, this nitrogen atom being further bound to an oxygen atom and not being part of nitro or nitroso groups
- C07C259/04—Compounds containing carboxyl groups, an oxygen atom of a carboxyl group being replaced by a nitrogen atom, this nitrogen atom being further bound to an oxygen atom and not being part of nitro or nitroso groups without replacement of the other oxygen atom of the carboxyl group, e.g. hydroxamic acids
- C07C259/10—Compounds containing carboxyl groups, an oxygen atom of a carboxyl group being replaced by a nitrogen atom, this nitrogen atom being further bound to an oxygen atom and not being part of nitro or nitroso groups without replacement of the other oxygen atom of the carboxyl group, e.g. hydroxamic acids having carbon atoms of hydroxamic groups bound to carbon atoms of six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C259/00—Compounds containing carboxyl groups, an oxygen atom of a carboxyl group being replaced by a nitrogen atom, this nitrogen atom being further bound to an oxygen atom and not being part of nitro or nitroso groups
- C07C259/12—Compounds containing carboxyl groups, an oxygen atom of a carboxyl group being replaced by a nitrogen atom, this nitrogen atom being further bound to an oxygen atom and not being part of nitro or nitroso groups with replacement of the other oxygen atom of the carboxyl group by nitrogen atoms, e.g. N-hydroxyamidines
- C07C259/18—Compounds containing carboxyl groups, an oxygen atom of a carboxyl group being replaced by a nitrogen atom, this nitrogen atom being further bound to an oxygen atom and not being part of nitro or nitroso groups with replacement of the other oxygen atom of the carboxyl group by nitrogen atoms, e.g. N-hydroxyamidines having carbon atoms of hydroxamidine groups bound to carbon atoms of six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D273/00—Heterocyclic compounds containing rings having nitrogen and oxygen atoms as the only ring hetero atoms, not provided for by groups C07D261/00 - C07D271/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D273/00—Heterocyclic compounds containing rings having nitrogen and oxygen atoms as the only ring hetero atoms, not provided for by groups C07D261/00 - C07D271/00
- C07D273/01—Heterocyclic compounds containing rings having nitrogen and oxygen atoms as the only ring hetero atoms, not provided for by groups C07D261/00 - C07D271/00 having one nitrogen atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D273/00—Heterocyclic compounds containing rings having nitrogen and oxygen atoms as the only ring hetero atoms, not provided for by groups C07D261/00 - C07D271/00
- C07D273/02—Heterocyclic compounds containing rings having nitrogen and oxygen atoms as the only ring hetero atoms, not provided for by groups C07D261/00 - C07D271/00 having two nitrogen atoms and only one oxygen atom
- C07D273/04—Six-membered rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
Abstract
Varios procedimientos para la obtencion de estos productos y su empleo para la lucha contra las pestes, así como productos intermedios y procedimientos para su obtencion. Reivindicacion 1: Compuestos de la formula (1), en la que A1 significa oxígeno o azufre; A2 significa oxígeno amino, aminoformilo o aminoacetilo; R1 significa hidrogeno, amino, hidroxi o significa alquilo con 1 a 6 átomos de carbono, alquenilo con 2 a 6 átomos de carbono, alquinilo con 2 a 6 átomos de carbono o cicloalquilo con 3 a 6 átomos de carbono, substituidos respectivamente en caso dado, una o varias veces, de forma igual o de formas diferentes, pudiéndose elegir los substituyentes independientemente entre sí, entre halogeno, ciano, nitro, hidroxi, alcoxi con 1 a 4 átomos de carbono, alquiltio con 1 a 4 átomos de carbono, alquilsulfinilo con 1 a 4 átomos de carbono, alquilsulfonilo con 1 a 4 átomos de carbono, (alcoxi con 1 a 4 átomos de carbono)carbonilo, alquilamino con 1 a 4 átomos de carbono, di-(alquilo con 1 a 4 átomos de carbono)amino, cicloalquilamino con 3 a 6 átomos de carbono o (alquilo con 1 a 4 átomos de carbono)cicloalquilamino con 3 a 6 átomos de carbono; R2 significan independientemente entre sí, alquilo con 1 a 6 átomos de carbono, alquenilo con 2 a 6 átomos de carbono, alquinilo con 2 a 6 átomos de carbono, cicloalquilo con 3 a 6 átomos de carbono, substituidos respectivamente en caso dado, una o varias veces, de forma igual o de formas diferentes, pudiéndose elegir los substituyentes independientemente entre sí, entre halogeno, ciano, nitro, alcoxi con 1 a 4 átomos de carbono, haloalcoxi con 1 a 4 átomos de carbono, alquiltio con 1 a 4 átomos de carbono, alquilsulfinilo con 1 a 4 átomos de carbono, alquilsulfonilo con 1 a 4 átomos de carbono, (alcoxi con 1 a 6 átomos de carbono)carbonilo, (alquilo con 1 a 6 átomos de carbono)carbonilo o trialquilsililo con 3 a 6 átomos de carbono; n significa desde 0 hasta 4; R3 significa hidrogeno, halogeno, ciano, nitro, alquilo con 1 a 4 átomos de carbono, haloalquilo con 1 a 4 átomos de carbono, alquenilo con 2 a 6 átomos de carbono, haloalquenilo con 2 a 6 átomos de carbono, alquinilo con 2 a 6 átomos de carbono, alcoxi con 1 a 4 átomos de carbono, haloalcoxi con 1 a 4 átomos de carbono, SF5, alquiltio con 1 a 4 átomos de carbono, alquilsulfinilo con 1 a 4 átomos de carbono, alquilsulfonilo con 1 a 4 átomos de carbono, haloalquiltio con 1 a 4 átomos de carbono, haloalquilsulfinilo con 1 a 4 átomos de carbono, haloalquilsulfonilo con 1 a 4 átomos de carbono, alquilamino con 1 a 4 átomos de carbono, di-(alquilo con 1 a 4 átomos de carbono)amino, cicloalquilamino con 3 a 6 átomos de carbono, (alcoxi con 1 a 4 átomos de carbono)imino, (alquilo con 1 a 4 átomos de carbono)(alcoxi con 1 a 4 átomos de carbono)imino, (haloalquilo con 1 a 4 átomos de carbono)(alcoxi con 1 a 4 átomos de carbono)imino o trialquilsililo con 3 a 6 átomos de carbono; R4 significa alquilo con 1 a 6 átomos de carbono, cicloalquilo con 3 a 6 átomos de carbono, haloalquilo con 1 a 6 átomos de carbono, halocicloalquilo con 1 a 6 átomos de carbono, alquenilo con 2 a 6 átomos de carbono, haloalquenilo con 2 a 6 átomos de carbono, alquinilo con 2 a 6 átomos de carbono, haloalquinilo con 2 a 6 átomos de carbono, alcoxi con 1 a 4 átomos de carbono, haloalcoxi con 1 a 4 átomos de carbono, alquiltio con 1 a 4 átomos de carbono, alquilsulfinilo con 1 a 4 átomos de carbono, alquilsulfonilo con 1 a 4 átomos de carbono, haloalquiltio con 1 a 4 átomos de carbono, haloalquilsulfinilo con 1 a 4 átomos de carbono, haloalquilsulfonilo con 1 a 4 átomos de carbono, halogeno, ciano, nitro o trialquilsililo con 3 a 6 átomos de carbono; R5 significa un anillo heteroaromático con 5 o 6 miembros, en caso dado, substituido una o varias veces, de forma igual o de formas diferentes, pudiéndose elegir los substituyentes independientemente entre sí, entre hidrogeno, alquilo con 1 a 6 átomos de carbono, alquenilo con 2 a 6 átomos de carbono, alquinilo con 2 a 6 átomos de carbono, cicloalquilo con 3 a 6 átomos de carbono, haloalquilo con 1 a 6 átomos de carbono, haloalquenilo con 2 a 6 átomos de carbono, haloalquinilo con 2 a 6 átomos de carbono, halocicloalquilo con 3 a 6 átomos de carbono, halogeno, CN, CO2H, CONH2, NO2, OH, alcoxi con 1 a 4 átomos de carbono, haloalcoxi con 1 a 4 átomos de carbono, alquiltio con 1 a 4 átomos de carbono, alquilsulfinilo con 1 a 4 átomos de carbono, alquilsulfonilo con 1 a 4 átomos de carbono, haloalquiltio con 1 a 4 átomos de carbono, haloalquilsulfinilo con 1 a 4 átomos de carbono, haloalquilsulfonilo con 1 a 4 átomos de carbono, alquilamino con 1 a 4 átomos de carbono, di-(alquilo con 1 a 4 átomos de carbono)amino, cicloalquilamino con 3 a 6 átomos de carbono, (alquilo con 1 a 6 átomos de carbono)carbonilo, (alcoxi con 1 a 6 átomos de carbono)carbonilo, (alquilo con 1 a 6 átomos de carbono)aminocarbonilo, di-(alquilo con 1 a 4 átomos de carbono)aminocarbonilo, trialquilsililo con 3 a 6 átomos de carbono, (alquilo con 1 a 4 átomos de carbono)(alcoxi con 1 a 4 átomos de carbono)imino o que pueden elegirse además, entre fenilo, benzoilo, fenoxi, anillos heteroaromáticos con 5 o 6 miembros o sistemas anulares heterobicíclicos, aromáticos, anillados con 8, con 9 o con10 miembros, pudiendo estar substituido cada uno de los aromatos, de los heteroaromatos o de los sistemas heterobicíclicos aromáticos, citados, en caso dado una o varias veces, de forma igual o de formas diferentes, pudiéndose elegir los substituyentes independientemente entre sí, entre alquilo con 1 a 6 átomos de carbono, alquenilo con 2 a 4 átomos de carbono, alquinilo con 2 a 4 átomos de carbono, cicloalquilo con 3 a 6 átomos de carbono, haloalquilo con 1 a 6 átomos de carbono, haloalquenilo con 2 a 6 átomos de carbono, haloalquinilo con 2 a 6 átomos de carbono, halocicloalquilo con 3 a 6 átomos de carbono, halogeno, CN, CO2H, CO2NH2, NO2, OH, alcoxi con 1 a 4 átomos de carbono, haloalcoxi con 1 a 4 átomos de carbono, alquiltio con 1 a 4 átomos de carbono, alquilsulfinilo con 1 a 4 átomos de carbono, alquilsulfonilo con 1 a 4 átomos de carbono, haloalquiltio con 1 a 4 átomos de carbono, haloalquilsulfinilo con 1 a 4 átomos de carbono, haloalquilsulfonilo con 1 a 4 átomos de carbono, (alquilo con 1 a 4 átomos de carbono)amino, di-(alquilo con 1 a 4 átomos de carbono)amino, cicloalquilamino con 3 a 6 átomos de carbono, (alquilo con 1 a 6 átomos de carbono)carbonilo, (alcoxi con 1 a 6 átomos de carbono)carbonilo, (alquilo con 1 a 6 átomos de carbono)aminocarbonilo, di-(alquilo con 2 a 8 átomos de carbono)aminocarbonilo, (alcoxi con 1 a 4 átomos de carbono)imino, (alquilo con 1 a 4 átomos de carbono)(alcoxi con 1 a 4 átomos de carbono)imino, (haloalquilo con 1 a 4 átomos de carbono)(alcoxi con 1 a 4 átomos de carbono)imino y trialquilsililo con 3 a 6 átomos de carbono; así como sus N-oxidos y sales.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102005044108A DE102005044108A1 (de) | 2005-09-15 | 2005-09-15 | Dioxazin- und Oxdiazin-substituierte Arylamide |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR056196A1 true AR056196A1 (es) | 2007-09-26 |
Family
ID=37442049
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP060103992A AR056196A1 (es) | 2005-09-15 | 2006-09-13 | Arilamidas substituidas por dioxazina y por oxidiazina |
Country Status (12)
| Country | Link |
|---|---|
| US (2) | US8062995B2 (es) |
| EP (1) | EP1926728B1 (es) |
| JP (1) | JP5124461B2 (es) |
| KR (1) | KR101410281B1 (es) |
| CN (1) | CN101287731B (es) |
| AR (1) | AR056196A1 (es) |
| AU (1) | AU2006291708A1 (es) |
| BR (1) | BRPI0616248A2 (es) |
| DE (1) | DE102005044108A1 (es) |
| ES (1) | ES2629081T3 (es) |
| TW (1) | TW200804361A (es) |
| WO (1) | WO2007031213A1 (es) |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2009001A1 (de) * | 2007-06-19 | 2008-12-31 | Bayer CropScience AG | Verfahren zur Herstellung von Dioxazin-Derivaten |
| EP2014658A1 (de) * | 2007-06-19 | 2009-01-14 | Bayer CropScience AG | Nicotinamid-Derivate und Verfahren zu deren Herstellung |
| WO2012007500A2 (de) | 2010-07-15 | 2012-01-19 | Bayer Cropscience Ag | Neue heterocyclische verbindungen als schädlingsbekämpfungsmittel |
| CN103958496B (zh) * | 2011-11-21 | 2017-05-24 | 巴斯夫欧洲公司 | 制备n‑取代的1h‑吡唑‑5‑甲酸盐化合物及其衍生物的方法 |
| CN104031037B (zh) * | 2014-06-23 | 2017-01-18 | 南京工业大学 | 一种含1，3，4‑噁二唑结构的甲酰苯胺类化合物及其制备方法与应用 |
| CN104370899A (zh) * | 2014-10-23 | 2015-02-25 | 南京工业大学 | 一种含1,2,4-噁二唑结构的甲酰苯胺类化合物及其制备方法与应用 |
| US9802927B2 (en) | 2015-06-10 | 2017-10-31 | Denali Therapeutics, Inc. | Oxadiazine compounds and methods of use thereof |
| CN107987068A (zh) * | 2017-12-08 | 2018-05-04 | 青岛清原化合物有限公司 | 一种二噁嗪衍生物及其制备方法、除草组合物和应用 |
| CN108250156B (zh) * | 2018-01-29 | 2021-07-09 | 华南农业大学 | 一种肉桂酸噁二嗪衍生物及其制备方法和应用 |
| EP3898620A1 (en) * | 2018-12-20 | 2021-10-27 | Bayer Aktiengesellschaft | Heterocyclyl pyridazine as fungicidal compounds |
| CA3186659A1 (en) * | 2020-06-10 | 2021-12-16 | Bayer Aktiengesellschaft | Azabicyclyl-substituted heterocycles as fungicides |
| CA3187297A1 (en) * | 2020-06-18 | 2021-12-23 | Bayer Aktiengesellschaft | Active compound combinations |
| JP2023532224A (ja) | 2020-06-18 | 2023-07-27 | バイエル、アクチエンゲゼルシャフト | 新規殺菌剤としてのオキサジアジニルピリダジン |
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| DE2651083A1 (de) | 1976-11-09 | 1978-05-18 | Hoechst Ag | Neue o-alkylierte hydroxylamine, verfahren zu ihrer herstellung und ihre verwendung |
| DE2820013A1 (de) | 1978-05-08 | 1979-11-22 | Hoechst Ag | Verfahren zur herstellung von o-alkylierten hydroxylaminen |
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| TWI283164B (en) | 2001-09-21 | 2007-07-01 | Du Pont | Anthranilamide arthropodicide treatment |
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| JP2003212834A (ja) | 2002-01-24 | 2003-07-30 | Nissan Chem Ind Ltd | アシルアンスラニル酸アミド化合物及び有害生物防除剤 |
| EP1546183A4 (en) | 2002-09-23 | 2008-06-18 | Du Pont | ISOLATION AND USE OF RYANODINE RECEPTORS |
| BR0314497A (pt) | 2002-10-04 | 2005-08-02 | Du Pont | Composto, método e composição para controle de praga invertebrada, composição spray, composição isca e dispositivo para controle de praga invertebrada |
| JP2005132727A (ja) * | 2003-10-28 | 2005-05-26 | Hokko Chem Ind Co Ltd | ジオキサジン誘導体および殺虫、殺ダニ剤 |
-
2005
- 2005-09-15 DE DE102005044108A patent/DE102005044108A1/de not_active Withdrawn
-
2006
- 2006-09-05 EP EP06777166.7A patent/EP1926728B1/de not_active Not-in-force
- 2006-09-05 CN CN2006800340100A patent/CN101287731B/zh not_active Expired - Fee Related
- 2006-09-05 JP JP2008530380A patent/JP5124461B2/ja not_active Expired - Fee Related
- 2006-09-05 AU AU2006291708A patent/AU2006291708A1/en not_active Abandoned
- 2006-09-05 BR BRPI0616248-7A patent/BRPI0616248A2/pt active Search and Examination
- 2006-09-05 US US11/992,006 patent/US8062995B2/en not_active Expired - Fee Related
- 2006-09-05 KR KR1020087008210A patent/KR101410281B1/ko not_active IP Right Cessation
- 2006-09-05 ES ES06777166.7T patent/ES2629081T3/es active Active
- 2006-09-05 WO PCT/EP2006/008637 patent/WO2007031213A1/de active Application Filing
- 2006-09-13 AR ARP060103992A patent/AR056196A1/es unknown
- 2006-09-14 TW TW095133959A patent/TW200804361A/zh unknown
-
2011
- 2011-11-09 US US13/292,517 patent/US8486934B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| US20120058891A1 (en) | 2012-03-08 |
| TW200804361A (en) | 2008-01-16 |
| AU2006291708A1 (en) | 2007-03-22 |
| US8062995B2 (en) | 2011-11-22 |
| EP1926728A1 (de) | 2008-06-04 |
| CN101287731A (zh) | 2008-10-15 |
| CN101287731B (zh) | 2012-02-08 |
| EP1926728B1 (de) | 2017-04-05 |
| WO2007031213A1 (de) | 2007-03-22 |
| DE102005044108A1 (de) | 2007-03-29 |
| JP2009512629A (ja) | 2009-03-26 |
| ES2629081T3 (es) | 2017-08-07 |
| BRPI0616248A2 (pt) | 2011-06-14 |
| KR20080046694A (ko) | 2008-05-27 |
| US8486934B2 (en) | 2013-07-16 |
| KR101410281B1 (ko) | 2014-06-23 |
| JP5124461B2 (ja) | 2013-01-23 |
| US20090143228A1 (en) | 2009-06-04 |
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